Wei Cong

672 total citations
32 papers, 473 citations indexed

About

Wei Cong is a scholar working on Molecular Biology, Cancer Research and Aerospace Engineering. According to data from OpenAlex, Wei Cong has authored 32 papers receiving a total of 473 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 10 papers in Cancer Research and 4 papers in Aerospace Engineering. Recurrent topics in Wei Cong's work include Cancer-related molecular mechanisms research (4 papers), Cancer, Hypoxia, and Metabolism (4 papers) and RNA modifications and cancer (4 papers). Wei Cong is often cited by papers focused on Cancer-related molecular mechanisms research (4 papers), Cancer, Hypoxia, and Metabolism (4 papers) and RNA modifications and cancer (4 papers). Wei Cong collaborates with scholars based in China, United Kingdom and Taiwan. Wei Cong's co-authors include Xiaolin Zhu, Zhengjun Yao, Lifang Lin, Shanmin Zhao, Wei Sun, Jing Xiao, Zhipeng Fan, Fu Wang, Shufang Cui and Pingze Zhang and has published in prestigious journals such as Food Chemistry, Biochemical and Biophysical Research Communications and Experimental Cell Research.

In The Last Decade

Wei Cong

29 papers receiving 461 citations

Peers

Wei Cong

PHYSI

Hiroki Ishii Japan

Yuheng Liu China

Wenhao Lu China

Jiarui Hu China

Zhixiang Lin Hong Kong

Aaron N. Johnson United States

Guannan Zhang China

Peta Bradbury Australia

Peter Zeller United States

Hiroki Ishii Japan

Wei Cong

145 ×0.6

65 ×0.7

38 ×0.8

31 ×0.7

40 ×1.0

PHYSI

Citations per year, relative to Wei Cong Wei Cong (= 1×) peers Hiroki Ishii

Countries citing papers authored by Wei Cong

Since Specialization

Citations

This map shows the geographic impact of Wei Cong's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Wei Cong with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wei Cong more than expected).

Fields of papers citing papers by Wei Cong

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wei Cong. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Wei Cong. The network helps show where Wei Cong may publish in the future.

Co-authorship network of co-authors of Wei Cong

This figure shows the co-authorship network connecting the top 25 collaborators of Wei Cong. A scholar is included among the top collaborators of Wei Cong based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Wei Cong. Wei Cong is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Cui, Yi, Xiaorui Li, Yiran Sun, et al.. (2025). Separation, characterization, AI screening, and bioactivities of marine bioactive peptides: A review. Food Chemistry. 495(Pt 1). 146312–146312.

Shi, Ce, Yingli Han, Kejia Hu, et al.. (2024). A metabolic atlas of blood cells in young and aged mice identifies uridine as a metabolite to rejuvenate aged hematopoietic stem cells. Nature Aging. 4(10). 1477–1492. 15 indexed citations

Hou, Yunlong, Chao Fang, Kun Ma, et al.. (2023). Bazi Bushen mitigates epigenetic aging and extends healthspan in naturally aging mice. Biomedicine & Pharmacotherapy. 160. 114384–114384. 24 indexed citations

Zeng, Xiangjun, Xia Li, Mi Shao, et al.. (2021). Integrated Single-Cell Bioinformatics Analysis Reveals Intrinsic and Extrinsic Biological Characteristics of Hematopoietic Stem Cell Aging. Frontiers in Genetics. 12. 745786–745786. 4 indexed citations

Cong, Wei, Qian Luo, Binsheng Wang, et al.. (2021). Generation of a FTO gene knockout human embryonic stem cell line using CRISPR/Cas9 editing. Stem Cell Research. 53. 102362–102362. 4 indexed citations

Luo, Qian, Wei Cong, Yan Long, et al.. (2021). Generation of an ELTD1 knockout human embryonic stem cell line by the iCRISPR/Cas9 system. Stem Cell Research. 53. 102350–102350.

Luo, Qian, Honghu Li, Wei Shan, et al.. (2021). Specific Blood Cells Derived from Pluripotent Stem Cells: An Emerging Field with Great Potential in Clinical Cell Therapy. Stem Cells International. 2021. 1–16. 5 indexed citations

Liu, Jianing, et al.. (2020). BAIAP2L2 promotes the progression of gastric cancer via AKT/mTOR and Wnt3a/β-catenin signaling pathways. Biomedicine & Pharmacotherapy. 129. 110414–110414. 13 indexed citations

Li, Xue, Xianwen Meng, Wei Cong, et al.. (2018). Dissecting LncRNA Roles in Renal Cell Carcinoma Metastasis and Characterizing Genomic Heterogeneity by Single-Cell RNA-seq. Molecular Cancer Research. 16(12). 1879–1888. 21 indexed citations

10.

Cong, Wei, Ji Wang, Rui Fu, et al.. (2018). The microbiota in the intestinal and respiratory tracts of naked mole-rats revealed by high-throughput sequencing. BMC Microbiology. 18(1). 89–89. 15 indexed citations

11.

Xiao, Bang, Li Li, Chang Xu, et al.. (2017). Transcriptome sequencing of the naked mole rat (Heterocephalus glaber) and identification of hypoxia tolerance genes. Biology Open. 6(12). 1904–1912. 7 indexed citations

12.

Wang, Fu, Yang Li, Xiaoshan Wu, et al.. (2017). Transcriptome analysis of coding and long non-coding RNAs highlights the regulatory network of cascade initiation of permanent molars in miniature pigs. BMC Genomics. 18(1). 148–148. 23 indexed citations

13.

Лю, Бо, Chao Liu, Wei Cong, et al.. (2017). Retinoid acid-induced microRNA-31-5p suppresses myogenic proliferation and differentiation by targeting CamkIIδ. Skeletal Muscle. 7(1). 8–8. 7 indexed citations

14.

Yang, Wenjing, Li Li, Guanghan Kan, et al.. (2017). Levels of Leydig cell autophagy regulate the fertility of male naked mole-rats. Oncotarget. 8(58). 98677–98690. 21 indexed citations

15.

Li, Nan, Yi Tang, Бо Лю, et al.. (2016). Retinoid acid-induced microRNA-27b-3p impairs C2C12 myoblast proliferation and differentiation by suppressing α-dystrobrevin. Experimental Cell Research. 350(2). 301–311. 13 indexed citations

16.

Zhao, Shanmin, Li Li, Shiyong Wang, et al.. (2016). H2O2 treatment or serum deprivation induces autophagy and apoptosis in naked mole-rat skin fibroblasts by inhibiting the PI3K/Akt signaling pathway. Oncotarget. 7(51). 84839–84850. 28 indexed citations

17.

Wang, Fu, Jing Xiao, Wei Cong, et al.. (2014). Stage-specific differential gene expression profiling and functional network analysis during morphogenesis of diphyodont dentition in miniature pigs, Sus Scrofa. BMC Genomics. 15(1). 103–103. 20 indexed citations

18.

Diao, Xuehong, et al.. (2010). MicroRNAs target gene and signaling pathway by bioinformatics analysis in the cardiac hypertrophy. Biochemical and Biophysical Research Communications. 397(3). 380–385. 22 indexed citations

19.

Zhu, Xiaolin, et al.. (2009). Microstructure and corrosion resistance of Fe-Al intermetallic coating on 45 steel synthesized by double glow plasma surface alloying technology. Transactions of Nonferrous Metals Society of China. 19(1). 143–148. 41 indexed citations

20.

Cong, Wei, et al.. (1992). Studies on the clinical significance of the clonal origins of recurrent hepatocellular carcinoma.. PubMed. 7(2). 101–4. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact